A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002032



Internal ID19091249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:144129913..144346626hg38UCSC Ensembl
Innerchr3:143848755..144065468hg19UCSC Ensembl
Innerchr3:145331445..145548158hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38216714
hg19216714
hg18216714
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3606132
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1002032
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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